Study identifier:MI-CP124-S2
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of MEDI-524, a Humanized Enhanced Potency Monoclonal Antibody Against Respiratory Syncytial Virus (RSV), in Children with Hemodynamically Significant Congenital Heart Disease
Congenital Heart Disease
Phase 2
No
-
All
1236
Interventional
0 Months - 24 Months
Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Prevention
Verified 01 Feb 2012 by MedImmune, LLC
MedImmune, LLC
-
The primary goal was to describe the safety of the investigational product when given monthly to prevent serious respiratory infection among children with significant heart disease.
The primary objective was to describe the safety and tolerability of motavizumab when given monthly as prophylaxis against serious RSV infection among children with hemodynamically significant congenital heart disease.
Location
Location
Paris, France, 75019
Location
Bordeaux, France, 33076
Location
Strasbourg, France, 67098
Location
Le Plessis Robinson, France, 93250
Location
Vandoeuvre les Nancy, France, 54511
Location
Reims, France, 51092
Location
Dijon, France, 21034
Location
Marseille, France, 13385
Arms | Assigned Interventions |
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Experimental: Motavizumab Motavizumab was administered as an intramuscular injection at 15 mg/kg every 30 days during the RSV season for a maximum of 5 scheduled doses. Additionally, children who underwent cardiac surgery with cardiopulmonary bypass through Study Day 150 were to receive a protocol-specified replacement dose of study drug immediately following the surgery when determined by the physician to be medically stable for an IM injection. | Biological/Vaccine: Motavizumab 15 mg/kg IM administered at monthly intervals Other Name: Medi-524 |
Active Comparator: Pailvizumab Palivizumab was administered as an intramuscular injection at 15 mg/kg every 30 days during the RSV season for a maximum of 5 scheduled doses. Additionally, children who underwent cardiac surgery with cardiopulmonary bypass through Study Day 150 were to receive a protocol-specified replacement dose of study drug immediately following the surgery when determined by the physician to be medically stable for an IM injection. | Biological/Vaccine: Palivizumab 15 mg/kg IM administered at monthly intervals Other Name: Synagis |
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